JP2509345B2 - Fluorine rubber vulcanizing composition having high tensile strength - Google Patents
Fluorine rubber vulcanizing composition having high tensile strengthInfo
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- JP2509345B2 JP2509345B2 JP25892989A JP25892989A JP2509345B2 JP 2509345 B2 JP2509345 B2 JP 2509345B2 JP 25892989 A JP25892989 A JP 25892989A JP 25892989 A JP25892989 A JP 25892989A JP 2509345 B2 JP2509345 B2 JP 2509345B2
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Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明はフッ素ゴムの新規な加硫組成物に関する。TECHNICAL FIELD The present invention relates to a novel vulcanizing composition of fluororubber.
フッ素ゴム加硫物は、優れた耐熱性、耐油性、耐薬品
性などを有していることから、各種の工業分野、例えば
自動車、船舶、航空機、油圧機器、一般機械工業、公害
関連部門などにおいて、O−リング、ガスケット、オイ
ルシール、ダイヤフラム、ホース、ロール、シート材な
どとして広く用いられている。しかしながら、フッ素ゴ
ム加硫物は引張強度が劣るため家庭用クーラー、カーエ
アコン、冷蔵庫、冷凍機等のパッキンして使用する場
合、フレオンによって膨潤した状態のまま圧力が急激に
変化すると割れが発生しシール性に問題が起こるケース
が多い。Fluorinated rubber vulcanizates have excellent heat resistance, oil resistance, chemical resistance, etc., so they are used in various industrial fields such as automobiles, ships, aircraft, hydraulic equipment, general machinery industry, pollution-related departments, etc. Are widely used as O-rings, gaskets, oil seals, diaphragms, hoses, rolls, sheet materials and the like. However, fluorinated rubber vulcanizates have poor tensile strength, so when used as packing for household coolers, car air conditioners, refrigerators, refrigerators, etc., cracks will occur if the pressure changes rapidly while still swollen by freon. In many cases, problems occur with the sealability.
本発明の目的は、極めて高い引張強度を達成し、かつ
従来のフッ素ゴム加硫物と同様に耐圧縮永久ひずみ性、
耐熱性、耐油性、耐薬品性に優れた加硫物を与え、しか
も容易に硬化しうる優れた加硫特性を有するフッ素ゴム
加硫組成物を提供することにある。The object of the present invention is to achieve extremely high tensile strength, and compression set resistance similar to conventional fluororubber vulcanizates,
It is an object of the present invention to provide a fluororubber vulcanization composition which gives a vulcanizate having excellent heat resistance, oil resistance and chemical resistance, and has excellent vulcanization characteristics that can be easily cured.
〔課題を解決するための手段〕 本発明者らは鋭意研究を重ねた結果、有機過酸化物、
共架橋剤、特定のカーボンブラックを特定の含フッ素エ
ラストマーに配合して成る組成物が前記目的に適合する
ことを見出し、この知見に基づいて本発明を完成するに
到った。[Means for Solving the Problems] As a result of intensive studies by the present inventors, an organic peroxide,
It has been found that a composition prepared by blending a co-crosslinking agent and a specific carbon black with a specific fluorine-containing elastomer meets the above-mentioned object, and based on this finding, the present invention has been completed.
すなわち、本発明は 1.(A)フッ化ビニリデン単位と少なくとも1種のフッ
素含有単量体とから成り、ヨウ素又は臭素を含有する極
限粘度(ml/g)が50〜100の範囲にある含フッ素エラス
トマー共重合体、(B)有機過酸化物、(C)共架橋
剤、(D)平均粒径30〜35μm、表面積70〜80m2/g、吸
油量1.2〜1.5ml/g、pH7.0〜7.7であるカーボンブラック
を含有して成るフッ素ゴム加硫組成物である。That is, the present invention comprises 1. (A) a vinylidene fluoride unit and at least one fluorine-containing monomer, and iodine or bromine-containing intrinsic viscosity (ml / g) in the range of 50 to 100. Fluoroelastomer copolymer, (B) organic peroxide, (C) co-crosslinking agent, (D) average particle size 30 to 35 μm, surface area 70 to 80 m 2 / g, oil absorption 1.2 to 1.5 ml / g, pH 7. A fluororubber vulcanizing composition containing 0 to 7.7 carbon black.
さらに本発明の好ましい実施態様としては 2.含フッ素エラストマー共重合体が、40〜85モル%のフ
ッ化ビニリデン単位を含有する前記第1項記載のフッ素
ゴム加硫組成物 3.含フッ素エラストマー共重合体がフッ化ビニリデン単
位と少なくとも1種のフッ素含有単量体とから成り、ヨ
ウ素を含有する極限粘度(ml/g)が50〜100の範囲にあ
る前記第1項記載のフッ素ゴム加硫組成物 4.共架橋剤がトリアリルイソシアヌレートである前記第
1項記載のフッ素ゴム加硫組成物などが挙げられる。Furthermore, as a preferred embodiment of the present invention, 2. The fluoroelastomer vulcanization composition according to the above 1, wherein the fluoroelastomer copolymer contains 40 to 85 mol% of vinylidene fluoride units. The fluororubber vulcanizate according to claim 1, wherein the polymer comprises vinylidene fluoride units and at least one fluorine-containing monomer, and the iodine-containing intrinsic viscosity (ml / g) is in the range of 50 to 100. Composition 4. The fluororubber vulcanization composition as described in the above item 1 in which the co-crosslinking agent is triallyl isocyanurate, etc. may be mentioned.
本発明のフッ素ゴム加硫組成物において(A)成分と
して用いる、フッ化ビニリデン単位と少なくとも1種の
フッ素含有単量体とから成り、ヨウ素又は臭素を含有す
る含フッ素エラストマー共重合体は、特公昭54−1585
号、特公昭63−41928号及び特開昭60−221409号公報に
開示されている。The fluorine-containing elastomer copolymer containing vinylidene fluoride units and at least one fluorine-containing monomer and containing iodine or bromine, which is used as the component (A) in the fluororubber vulcanizing composition of the present invention, is Kosho 54-1585
JP-B-63-41928 and JP-A-60-221409.
少なくとも1種のフッ素含有単量体単位としては、例
えばヘキサフルオロプロペン、ペンタフルオロプロペ
ン、テトラフルオロエチレン、ツリフルオロエチレン、
クロロトリフルオロエチレン、ジクロロジフルオロエチ
レン、ブロモトリフルオロエチレン、4−ブロモ−3,3,
4,4−テトラフルオロブテン−1、フッ素化ビニルエー
テル類、フッ素化アルキルビニルエーテル類などが挙げ
られる。この含フッ素エラストマーの極限粘度(ml/g)
が50〜100の範囲にあるのは、極限粘度(ml/g)が50未
満では本発明の目的である高い引張強さが得られず、10
0を超えると十分な架橋密度が得られないため圧縮永久
ひずみの悪化を招くためである。Examples of the at least one fluorine-containing monomer unit include hexafluoropropene, pentafluoropropene, tetrafluoroethylene, trifluoroethylene,
Chlorotrifluoroethylene, dichlorodifluoroethylene, bromotrifluoroethylene, 4-bromo-3,3,
4,4-tetrafluorobutene-1, fluorinated vinyl ethers, fluorinated alkyl vinyl ethers and the like can be mentioned. Intrinsic viscosity (ml / g) of this fluorine-containing elastomer
Is in the range of 50 to 100 when the intrinsic viscosity (ml / g) is less than 50, the high tensile strength, which is the object of the present invention, cannot be obtained.
This is because if it exceeds 0, a sufficient crosslink density cannot be obtained and the compression set is deteriorated.
また、(A)成分の含フッ素エラストマー共重合体の
例としては、フッ化ビニリデン−ヘキサフルオロプロペ
ン共重合体、フッ化ビニリデン−ヘキサフルオロプロペ
ン−テトラフルオロエチレン共重合体、フッ化ビニリデ
ン−ヘキサフルオロプロペン−テトラフルオロエチレン
−4−ブロモ−3,3,4、4−テトラフルオロブテン−1
共重合体などが挙げられる。In addition, examples of the fluorine-containing elastomer copolymer of the component (A) include vinylidene fluoride-hexafluoropropene copolymer, vinylidene fluoride-hexafluoropropene-tetrafluoroethylene copolymer, vinylidene fluoride-hexafluoro. Propene-tetrafluoroethylene-4-bromo-3,3,4,4-tetrafluorobutene-1
Examples thereof include copolymers.
これらの共重合体の加硫成形に際しては、加熱で分解
した有機過酸化物によってポリマー中のヨウ素又は臭素
が外れてラジカルとなり、共架橋剤を仲介して架橋する
ことが知られている。During vulcanization molding of these copolymers, it is known that the organic peroxide decomposed by heating removes iodine or bromine in the polymer to form a radical, which is mediated by a co-crosslinking agent to crosslink.
(B)成分の有機過酸化物の例としては、加硫条件下で
パーオキサイドラジカルを発生するものであれば良く、
例えば1,1−ビス(t−ブチルパーオキシ)−3,3,5−ト
リメチルシクロヘキサン、2,5−ジメチルヘキサン−2,5
−ジヒドロキシパーオキシド、ジ−t−ブチルパーオキ
シド、t−ブチルクミルパーオキシド、ジクミルパーオ
キシド、a,a′−ビス(t−ブチルパーオキシ)−p−
ジイソプロピルベンゼン、2,5−ジメチル−2,5−ジ(t
−ブチルパーオキシ)ヘキシン、2,5−ジメチル−2,5−
ジ(t−ブチルパーオキシ)ヘキシン−3、ベンゾイル
パーオキシド、t−ブチルパーオキシベンゼン、2,5−
ジメチル−2,5−ジ(ベンゾイルパーオキシ)ヘキサ
ン、t−ブチルパーオキシマレイン酸、t−ブチル−オ
キシイソプロピルカーボネイトなどが挙げられる。As an example of the organic peroxide as the component (B), any organic peroxide capable of generating a peroxide radical under vulcanization conditions may be used.
For example, 1,1-bis (t-butylperoxy) -3,3,5-trimethylcyclohexane, 2,5-dimethylhexane-2,5
-Dihydroxy peroxide, di-t-butyl peroxide, t-butyl cumyl peroxide, dicumyl peroxide, a, a'-bis (t-butylperoxy) -p-
Diisopropylbenzene, 2,5-dimethyl-2,5-di (t
-Butylperoxy) hexyne, 2,5-dimethyl-2,5-
Di (t-butylperoxy) hexyne-3, benzoyl peroxide, t-butylperoxybenzene, 2,5-
Examples thereof include dimethyl-2,5-di (benzoylperoxy) hexane, t-butylperoxymaleic acid, t-butyl-oxyisopropyl carbonate and the like.
(C)成分の共架橋剤としては、例えばトリアリルシア
ヌレート、トリアリルイソシアヌレート、トリメタリル
イソシアヌレート、トリアクリルホルマール、トリアリ
ルトリメリテート、N,N′−m−フエニレンビスマレイ
ミド、ジアリルフタレート、テトラアリルテレフタール
アミド、トリス(ジアリルアミン)−s−トリアジン、
亜燐酸トリアリル、N,N−ジアリルアクリルアミドなど
が挙げられ、特に好ましい共架橋剤はトリアリルイソシ
アヌレートである。Examples of the co-crosslinking agent as the component (C) include triallyl cyanurate, triallyl isocyanurate, trimethallyl isocyanurate, triacrylic formal, triallyl trimellitate, N, N'-m-phenylene bismaleimide, diallyl. Phthalate, tetraallyl terephthalamide, tris (diallylamine) -s-triazine,
Examples thereof include triallyl phosphite, N, N-diallyl acrylamide and the like, and a particularly preferable co-crosslinking agent is triallyl isocyanurate.
(D)成分のカーボンブラックは、平均粒径30〜35μ
m、表面積70〜80m2/g、吸油量1.2〜1.5ml/g、pH7.0〜
7.7であり、例えばMAFカーボンブラックが挙げられる。
MAFカーボンブラックの商品名としては東海カーボン
(株)製品「シースト116」、旭カーボン(株)製品
「旭#60H」などがある。The carbon black of component (D) has an average particle size of 30 to 35 μm.
m, surface area 70-80 m 2 / g, oil absorption 1.2-1.5 ml / g, pH 7.0-
7.7, for example MAF carbon black.
Product names of MAF carbon black include Tokai Carbon Co., Ltd. product “Seast 116” and Asahi Carbon Co., Ltd. product “Asahi # 60H”.
本発明のフッ素ゴム加硫組成物における前記各成分の
配合割合については、通常(A)成分100重量部に対し
て、(B)成分0.1〜5重量部、好ましくは0.5〜3重量
部、(C)成分0.1〜10重量部、好ましくは0.5〜5重量
部、(D)成分1〜50重量部、好ましくは5〜30重量部
である。なお(B)成分がこの範囲にあるのは、0.1重
量部未満では十分な硬化速度が得られず、5を超えると
加硫物の常態物性が低下するためであり、(C)成分が
この範囲にあるのは、0.1重量部未満では均一な加硫物
が得られず、10重量部を超えると加硫物の常態物性が低
下するためであり、(D)成分がこの範囲にあるのは、
1重量部未満では高い引張強さが得られず、50重量部を
超えると加硫物の弾性体としての特性が大幅に低下する
ためである。Regarding the compounding ratio of each of the above components in the fluororubber vulcanizing composition of the present invention, usually 0.1 to 5 parts by weight, preferably 0.5 to 3 parts by weight, of (B) component, relative to 100 parts by weight of (A) component, ( Component (C) is 0.1 to 10 parts by weight, preferably 0.5 to 5 parts by weight, and component (D) is 1 to 50 parts by weight, preferably 5 to 30 parts by weight. The reason why the component (B) is in this range is that if the amount is less than 0.1 parts by weight, a sufficient curing rate cannot be obtained, and if it exceeds 5, the normal physical properties of the vulcanizate are deteriorated. The range is because if less than 0.1 part by weight, a uniform vulcanized product cannot be obtained, and if it exceeds 10 parts by weight, the physical properties of the vulcanized product deteriorate, and the component (D) is in this range. Is
This is because if it is less than 1 part by weight, high tensile strength cannot be obtained, and if it exceeds 50 parts by weight, the properties of the vulcanizate as an elastic body are significantly deteriorated.
さらに本発明のフッ素ゴム加硫組成物においては、必
要に応じ、他の成分、例えば本発明の請求範囲以外のカ
ーボンブラック、シリカ、クレー、ケイソウ土、炭酸カ
ルシウム、フッ化カルシウム、硫酸バリウムなどの充填
剤、加工助剤、可塑剤、着色剤、さらに酸化マグネシウ
ム、酸化鉛、酸化カルシウムなどの受酸剤を配合するこ
とができる。また、本発明の主旨を逸脱しない範囲であ
れば、従来公知の加硫剤や加硫促進剤を1種又は2種配
合してもよい。Further, in the fluororubber vulcanizing composition of the present invention, if necessary, other components such as carbon black, silica, clay, diatomaceous earth, calcium carbonate, calcium fluoride, barium sulfate, etc., other than those claimed in the present invention, Fillers, processing aids, plasticizers, colorants, and acid acceptors such as magnesium oxide, lead oxide and calcium oxide may be added. Further, one or two conventionally known vulcanizing agents or vulcanization accelerators may be blended within a range not departing from the gist of the present invention.
このようにして得られたフッ素ゴム加硫組成物は、常
法に従って加硫される。この加硫方法としては、例えば
解放型練りロール又は密閉式練りロール(バンバリーミ
キサー、加圧式ニーダー等)で混練後、型に入れ加圧し
て一次加硫し、次いで二次加硫する方法が挙げられる。
一般に、一次加硫の条件として温度120〜20℃、時間3
〜180分、圧力20〜150kg/m2の範囲が、二次加硫の条件
としては、温度120〜250℃、時間0〜48時間の範囲が採
用される。また、他の加硫手段として、射出又は押出し
などの予備成形をした後に加硫する方法、あるいはメチ
ルエチルケトン、アセトンなどのケトン類、エチルエー
テル、テトラヒドロフランなどのエーテル類などの1種
又は2種以上を媒体とする溶液もしくは分散液を調整
し、これで紙、繊維、フィルタ、シート、板、チュー
ブ、パイプ、タンク、大型容器その他の成形品の表面上
を被覆し加硫する方法などを用いることもできる。The fluororubber vulcanization composition thus obtained is vulcanized according to a conventional method. Examples of this vulcanization method include a method in which after kneading with an open-type kneading roll or a closed-type kneading roll (Banbury mixer, pressure kneader, etc.), the mixture is put into a mold and pressurized to perform primary vulcanization, and then secondary vulcanization. To be
Generally, the conditions for primary vulcanization are a temperature of 120 to 20 ° C and a time of 3
The range of 180 to 180 minutes and the pressure of 20 to 150 kg / m 2 and the range of the temperature of 120 to 250 ° C. and the time of 0 to 48 hours are adopted as the secondary vulcanization conditions. As other vulcanizing means, a method of vulcanizing after preforming such as injection or extrusion, or one or more of methyl ethyl ketone, ketones such as acetone, ethyl ether, ethers such as tetrahydrofuran, etc. may be used. It is also possible to use a method in which a solution or dispersion liquid as a medium is prepared, and then the surface of a paper, fiber, filter, sheet, plate, tube, pipe, tank, large container or other molded article is coated and vulcanized. it can.
本発明のフッ素ゴム加硫組成物は、極めて高い引張強
度を達成し、かつ従来のフッ素ゴム加硫物と同様に耐圧
縮永久ひずみ性、耐熱性、耐油性、耐薬品性に優れた加
硫物を与え、しかも容易に硬化しうる優れた加硫特性を
有している。従って、各種工業分野、例えば自動車、船
舶、航空機、油圧機器、一般機械工業、公害関連部門な
どにおいて,O−リング、ガスケット、オイルシール、ダ
イヤフラム、ホース、ロール、シート材などとして広く
使用できるばかりでなく、従来、フッ素ゴム加硫物の使
用が制限されていたフレオンと接する家庭用クーラー、
カーエアコン、冷蔵庫、冷凍機等のパッキンとしても使
用が可能であり、工業的価値は極めて高い。The fluororubber vulcanization composition of the present invention achieves extremely high tensile strength, and, like the conventional fluororubber vulcanizates, is vulcanized with excellent compression set resistance, heat resistance, oil resistance, and chemical resistance. It has excellent vulcanization characteristics that give a product and can be easily cured. Therefore, it can be widely used as O-rings, gaskets, oil seals, diaphragms, hoses, rolls, sheet materials, etc. in various industrial fields such as automobiles, ships, aircraft, hydraulic equipment, general machinery industry, and pollution-related departments. , A household cooler that comes into contact with Freon, which had been previously restricted in the use of fluororubber vulcanizates,
It can be used as packing for car air conditioners, refrigerators, refrigerators, etc., and has an extremely high industrial value.
次ぎに実施例により本発明をさらに詳細に説明する
が、本発明はこれらの例によってなんら限定されるもの
ではない。Next, the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples.
なお、加硫物の硬さはJIS−A、100%引張応力、引張
強さ、伸び、圧縮永久ひずみJIS K 6301に準じて測定し
た。また極限粘度(ml/g)は含フッ素エラストマーをメ
チルエチルケトンに溶解して0.1ml/gの濃度溶液を作成
し毛細管粘度計を用いて35℃で測定した。The hardness of the vulcanized product was measured according to JIS-A, 100% tensile stress, tensile strength, elongation, compression set JIS K 6301. The intrinsic viscosity (ml / g) was measured at 35 ° C. using a capillary viscometer by dissolving a fluoroelastomer in methyl ethyl ketone to prepare a 0.1 ml / g concentration solution.
さらにカーボンブラックの特性はつぎの測定法によっ
た。すなわち平均粒径は電子顕微鏡で測定(ASTM D 176
5)、表面積はASTM D 3037、pHはJIS K 6221 6.4.2、吸
油量はJIS K 6221 6.1.2A法である。Further, the characteristics of carbon black were determined by the following measuring methods. That is, the average particle size is measured by an electron microscope (ASTM D 176
5), surface area is ASTM D 3037, pH is JIS K 6221 6.4.2, oil absorption is JIS K 6221 6.1.2A method.
実施例1 組成がフッ化ビニリデン単位65モル%、ヘキサフルオ
ロプロペン単位15モル%、テトラフルオロエチレン単位
20モル%、極限粘度72ml/g、ヨウ素含量2000ppmの含フ
ッ素エラストマー100重量部を開放型練りロールに巻付
け、これに2,5−ジメチル−2,5−ジ(t−ブチルパーオ
キシ)ヘキサン1.5重量部、トリアリルイソシアヌレー
ト3重量部、シースト116 10重量部を練り込んだ後、そ
のまま一夜放置して熟成させた。Example 1 The composition has a vinylidene fluoride unit of 65 mol%, a hexafluoropropene unit of 15 mol%, and a tetrafluoroethylene unit.
100 parts by weight of a fluorine-containing elastomer having 20 mol%, an intrinsic viscosity of 72 ml / g and an iodine content of 2000 ppm was wound around an open-type kneading roll, and 2,5-dimethyl-2,5-di (t-butylperoxy) hexane was wrapped around this. After kneading 1.5 parts by weight, 3 parts by weight of triallyl isocyanurate, and 10 parts by weight of SAST 116, the mixture was left to stand overnight for aging.
その後、再練りを行なってから金型に入れ、温度160
℃でプレス加硫を10分間行い、シート及びJIS円柱に成
形した。Then, after kneading again, put it in the mold and
Press vulcanization was performed at ℃ for 10 minutes, and formed into a sheet and a JIS cylinder.
次いで金型から取り出し、温度180℃の空気循環式炉
内で4時間加熱して二次加硫を完結させ各種試験を行な
った。Then, it was taken out from the mold and heated in an air circulation type furnace at a temperature of 180 ° C. for 4 hours to complete the secondary vulcanization, and various tests were conducted.
このようにして得られた加硫成形物の常態物性、耐圧
縮永久ひずみ性を表1に示す。Table 1 shows the normal physical properties and compression set resistance of the vulcanized molded product thus obtained.
実施例2 シースト116の配合量を15重量部にする以外は実施例
1と同様にして加硫成形物を調整し、各種試験を行なっ
た。結果を表1に示す。Example 2 A vulcanized molded product was prepared and various tests were carried out in the same manner as in Example 1 except that the amount of the cast 116 was changed to 15 parts by weight. The results are shown in Table 1.
実施例3 シースト116の配合量を20重量部にする以外は実施例
1と同様にして加硫成形物を調整し各種試験を行なっ
た。結果を表1に示す。Example 3 A vulcanized molded product was prepared and various tests were conducted in the same manner as in Example 1 except that the compounding amount of the cast 116 was changed to 20 parts by weight. The results are shown in Table 1.
実施例4 シースト116の配合量を30重量部にし、プレス加硫時
間を12分にする以外は実施例1と同様にして加硫成形物
を調整し各種試験を行なった。結果を表1に示す。Example 4 A vulcanized molded product was prepared and various tests were carried out in the same manner as in Example 1 except that the amount of the cast 116 was 30 parts by weight and the press vulcanization time was 12 minutes. The results are shown in Table 1.
実施例5 組成がフッ化ビニリデン単位55モル%、ヘキサフルオ
ロプロペン単位25モル%、テトラフルオロエチレン単位
20モル%、極限粘度52ml/g、ヨウ素含量1600ppmを使用
する以外は実施例3と同様にして加硫成形物を調整し各
種試験を行なった。結果を表1に示す。Example 5 The composition has a vinylidene fluoride unit of 55 mol%, a hexafluoropropene unit of 25 mol%, and a tetrafluoroethylene unit.
A vulcanized molded product was prepared and various tests were conducted in the same manner as in Example 3 except that 20 mol%, an intrinsic viscosity of 52 ml / g and an iodine content of 1600 ppm were used. The results are shown in Table 1.
比較例1 組成がフッ化ビニリデン単位65モル%、ヘキサフルオ
ロプロペン単位15モル%、テトラフルオロエチレン単位
20モル%、極限粘度48ml/g、ヨウ素含量4200ppmの含フ
ッ素エラストマーを使用する以外は実施例3と同様にし
て加硫成形物を調整し各種試験を行なった。結果を表1
に示す。Comparative Example 1 Composition: Vinylidene fluoride unit 65 mol%, Hexafluoropropene unit 15 mol%, Tetrafluoroethylene unit
A vulcanized molded product was prepared and various tests were conducted in the same manner as in Example 3 except that a fluorine-containing elastomer having 20 mol%, an intrinsic viscosity of 48 ml / g and an iodine content of 4200 ppm was used. The results are shown in Table 1.
Shown in
比較例2 シースト116の代わりに東海カーボン(株)製品シー
ストS(SRFカーボンブラック、平均粒径58〜94μm、
表面積25〜30m2/g、吸油量0.7〜0.9ml/g、pH7.5〜9.0)
15重量部を配合する以外は実施例1と同様にして加硫成
形物を調整し、各種試験を行なった。結果を表1に示
す。Comparative Example 2 Tokai Carbon Co., Ltd. product Seast S (SRF carbon black, average particle size 58 to 94 μm, instead of Seast 116,
Surface area 25-30 m 2 / g, oil absorption 0.7-0.9 ml / g, pH 7.5-9.0)
A vulcanized molded product was prepared and various tests were conducted in the same manner as in Example 1 except that 15 parts by weight was compounded. The results are shown in Table 1.
比較例3 シースト116の代わりにキヤンカーブ社製品サーマッ
クス(MTカーボンブラック平均粒径450〜556μm、表面
積5〜7m2/g、吸油量0.3〜0.5ml/g、pH9〜11)20重量
部を配合する以外は実施例1と同様にして加硫成形物を
調整し各種試験を行なった。結果を表1に示す。Comparative Example 3 20 parts by weight of Cyanmax's product THERMAX (MT carbon black average particle size 450 to 556 μm, surface area 5 to 7 m 2 / g, oil absorption 0.3 to 0.5 ml / g, pH 9 to 11) was blended instead of Seast 116. A vulcanized molded product was prepared and various tests were carried out in the same manner as in Example 1 except that the above was performed. The results are shown in Table 1.
〔発明の効果〕 本発明のフッ素ゴム加硫組成物は、極めて高い引張強
度を達成し、かつ従来のフッ素ゴム加硫物と同様に耐圧
縮永久ひずみ性、耐熱性、耐油性、耐薬品性に優れた加
硫物を与え、しかも容易に硬化しうる優れた加硫物性を
有している。 [Effects of the Invention] The fluororubber vulcanization composition of the present invention achieves extremely high tensile strength, and has compression set resistance, heat resistance, oil resistance, and chemical resistance similar to conventional fluororubber vulcanizates. It has excellent vulcanizate properties and can be easily cured.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭63−308008(JP,A) 特開 昭61−55138(JP,A) 特開 昭56−86948(JP,A) 特開 昭54−129049(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (56) Reference JP-A-63-308008 (JP, A) JP-A-61-55138 (JP, A) JP-A-56-86948 (JP, A) JP-A-54- 129049 (JP, A)
Claims (1)
1種のフッ素含有単量体とから成り、ヨウ素又は臭素を
含有する極限粘度(ml/g)が50〜100の範囲にある含フ
ッ素エラストマー共重合体、(B)有機過酸化物、
(C)共架橋剤、(D)平均粒径30〜35μm、表面積70
〜80m2/g、吸油量1.2〜1.5ml/g、pH7.0〜7.7であるカー
ボンブラックを含有して成るフッ素ゴム加硫組成物。1. A fluorine-containing elastomer comprising (A) a vinylidene fluoride unit and at least one fluorine-containing monomer and containing iodine or bromine and having an intrinsic viscosity (ml / g) in the range of 50 to 100. Copolymer, (B) organic peroxide,
(C) Co-crosslinking agent, (D) Average particle size 30 to 35 μm, surface area 70
A fluororubber vulcanizing composition containing carbon black having a viscosity of -80 m 2 / g, an oil absorption of 1.2-1.5 ml / g and a pH of 7.0-7.7.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25892989A JP2509345B2 (en) | 1989-10-05 | 1989-10-05 | Fluorine rubber vulcanizing composition having high tensile strength |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25892989A JP2509345B2 (en) | 1989-10-05 | 1989-10-05 | Fluorine rubber vulcanizing composition having high tensile strength |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03122153A JPH03122153A (en) | 1991-05-24 |
JP2509345B2 true JP2509345B2 (en) | 1996-06-19 |
Family
ID=17327005
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25892989A Expired - Lifetime JP2509345B2 (en) | 1989-10-05 | 1989-10-05 | Fluorine rubber vulcanizing composition having high tensile strength |
Country Status (1)
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---|---|
JP (1) | JP2509345B2 (en) |
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JP5254889B2 (en) * | 2009-06-19 | 2013-08-07 | タイガースポリマー株式会社 | Highly conductive fluororubber composition containing carbon black |
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WO2012026553A1 (en) | 2010-08-25 | 2012-03-01 | ダイキン工業株式会社 | Fluororubber composition |
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WO2012026555A1 (en) * | 2010-08-25 | 2012-03-01 | ダイキン工業株式会社 | Fluororubber molded article |
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US10000619B2 (en) | 2011-08-25 | 2018-06-19 | Daikin Industries, Ltd. | Diaphragm |
JP5862762B2 (en) | 2012-01-20 | 2016-02-16 | ダイキン工業株式会社 | Fluororubber composition and method for producing the same |
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WO2013125736A1 (en) | 2012-02-24 | 2013-08-29 | Daikin Industries, Ltd. | Fluororubber composition |
US11898661B2 (en) * | 2012-02-24 | 2024-02-13 | Daikin Industries, Ltd. | Fluororubber composition |
-
1989
- 1989-10-05 JP JP25892989A patent/JP2509345B2/en not_active Expired - Lifetime
Cited By (2)
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Also Published As
Publication number | Publication date |
---|---|
JPH03122153A (en) | 1991-05-24 |
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